Abstract: Medical articles including an absorbent layer, a backing layer and an optional liquid permeable facing layer are disclosed. The construction of the medical article is such that volumetric expansion of the absorbent layer is allowed in directions parallel to the surface of the backing layer as the absorbent layer absorbs moisture. The medical article may include a debonding agent located between the absorbent layer and the backing layer. The absorbent layer is operably attached to the backing layer. When the absorbent layer absorbs moisture, e.g., wound exudate, at least a portion of the absorbent layer detaches from the backing layer such that the absorbent layer can expand and move relative to the backing. The debonding agent facilitates this change from attachment to detachment of the absorbent layer to the backing.

Abstract: A scent emitting patch remains securely attached to the skin of a wearer. The patch has an external top layer and backing layer with a skin-contacting portion. The skin-contacting segment contains an adhesive. At least one reservoir comprising pockets or microcapsules containing a scent is disposed in at least one portion of the backing layer. These pockets or microcapsules are operative to rupture upon application of pressure or scratching by the patch wearer. Upon rupture, scent is delivered to the skin to emit aroma. Pockets containing the scent are formed in the backing layer. Microcapsules, if present, are preferably incorporated in the adhesive. Scent is released at the skin-contact interface when pressure is applied to rupture the pockets or microcapsules, permitting controlled release at the wearer's election.

Abstract: A wound treatment for use during phototherapy treatment of a wound includes a pliable optical component adapted to be applied over the wound and to direct light rays during phototherapy treatment, and a bandage for securing the Fresnel lens over the wound. The optical component may be configured to direct light rays toward a perimeter edge of the wound. A wound treatment kit for phototherapy treatment of a wound includes a package and a sterile, pliable optical component in the package. The optical component is removable from the sterile package and is placed over the wound during the phototherapy treatment. The optical component directs light rays toward a selected area of the wound during phototherapy treatment.

Abstract: An adhesive patch configured to attach an ostomy appliance to a patient includes a peripheral rim disposed around a central hole that is attachable to a stoma of the patient; and a band of adhesive extending from the peripheral rim to an inner border of the adhesive patch and having a pattern of curvilinear indentations extending to the peripheral rim of the patch.

Abstract: A bandage that facilitates the removal of the bandage from the skin is shown and described. The bandage comprises a selectively releasable adhesion reducing material contained in structures such as a selectively rupturable reservoir or a selectively deformable synthetic or natural matrix. When the adhesion reducing material is released from the reservoir, it contacts the bandage's skin adhesive and reduces its adhesion to the skin.

Abstract: According to the various features, characteristics and embodiments of the present invention which will become apparent as the description thereof proceeds, the present invention provides attachable grip enhancers for general use, as well as in playing the game of various sports, that could be attached to an individual, and uses and methods thereof. The present invention and its embodiments can, among other things, enhance the overall performance in arm tasks conducted by the wrist, forearm and/or bicep areas, as well as hand tasks.

Abstract: Devices, bandages, kits and methods are described that can control or regulate the mechanical environment of a wound to ameliorate scar and/or keloid formation. The mechanical environment of a wound includes stress, strain, and any combination of stress and strain. The control of a wound's mechanical environment can be active, passive, dynamic, or static. The devices are configured to be removably secured to a skin surface in proximity to the wound site and shield the wound from endogenous and/or exogenous stress.

Abstract: The field of the invention is that of articles adhesive to the skin for medical or paramedical use. The invention relates to an article adhesive to the skin.

Abstract: Apparatus and associated methods for a wound valve assembly provide an annular space extending radially around a central portion of a valve, which valve acts to substantially relieve pressure build up in a thoracic cavity when applied to a thoracic wound. In an illustrative example, the valve assembly may form an annular space that extends radially in all directions around a check valve. In some examples, gasses and exudates may flow substantially radially and/or parallel to the patient's local body. Various embodiments may advantageously provide open fluid communication for the gasses and exudates escaping from the wound when the valve assembly is partially covered (e.g., body armor, clothing, blankets), or when the patient may be lying down on the side of the body with the wound, for example.

Abstract: A vacuum bandage is provided for use with a wound having a wound surface. The bandage is connectable to a vacuum source and includes a wound dressing member having a wound contacting surface, a top surface, and a port configured for communication with the vacuum source. The wound dressing member further includes holes in the wound contacting surface configured for communication with the wound surface of the wound and a passageway between the port and each hole. The vacuum bandage further includes a pack adjacent to the top surface of the member. The pack may include an aperture positioned about the port.

Abstract: A hemostatic device for promoting the dotting of blood includes a gauze substrate, a clay material disposed on the gauze substrate, and also a polyol such as glycerol or the like disposed on the gauze substrate to bind the clay material. When the device is used to treat a bleeding wound, at least a portion of the clay material comes into contact with blood emanating from the wound to cause the clotting. A bandage that can be applied to a bleeding wound to promote the clotting of blood includes a flexible substrate and a gauze substrate mounted thereon. The gauze substrate includes a clay material and a polyol. A hemostatic sponge also includes a gauze substrate and a dispersion of hemostatic material and a polyol on a first surface of the substrate.

Abstract: A dressing product includes a thin film dressing sheet, one first surface of which is coated with an adhesive, such as a pressure sensitive hydrocolloid adhesive, which is applicable to an anatomical surface of a human. A carrier system, which provides a support for the dressing sheet, defines a gripping section for handling of the carrier system. The carrier system may include one or more foil members and supporting sheets for facilitating application and for providing a non-touch application system, i.e., a system which may be handled by an operator without the operator touching the dressing sheet or at least the adhesive surface. A protective sheet having an opening for application of a pharmaceutical product to the adhesive prior to application of the dressing sheet is disclosed.

Abstract: A pressure-sensitive adhesive bandage with a magnetically-released triggering mechanism is provided. The pressure-sensitive bandage may include a backing for providing support for the pressure-sensitive adhesive bandage. Additionally, the pressure-sensitive bandage may include a pressure-sensitive adhesive applied to the backing, which may include microcapsules. The microcapsules may include a silica-based shell, a core confined within the silica-based shell that includes oil, and a plurality of magnetic particles that may be positioned in at least one of the silica-based shell and the core. The plurality of magnetic particles may be configured to cause the silica-based shell to release the oil from the core when a magnetic force is exerted on the plurality of magnetic particles.

Abstract: An applicator (1) for applying an article (2) to the skin (3) of a patient comprising a liner (4), an article carrying layer (5) and an applicator layer (6), and where the article carrying layer (5) has a bottom (7) and a top (8) surface, both being delimited by the periphery (9) of the carrying layer (5), and where the bottom surface (7) comprises an article carrying area (10), where the article (2) is fixed to the carrying layer (5), and an adhesive area (11) being releasably adhered to a surface (12) on the liner (4) by means of a first adhesive, and where the applicator layer (6) has a surface (13) being releasably adhered to only a first part (14) of the top surface (8) of the article carrying layer (5) and its periphery (9), by means of a second adhesive, and where the first and the second adhesives are selected so that, when the applicator layer (6) is pulled away from the liner (4) in an area where the applicator layer (6) and the second adhesive covers the first part of the periphery of the article c

Abstract: A method for making a net patterned adhesive layer by a mold, and a wound dressing having a net patterned adhesive layer.

Abstract: An adhesive wafer for an ostomy faceplate or wound dressing comprising a backing layer, said backing layer having one surface facing the skin, said surface comprising a first and a second adhesive zone being separated from each others by a void volume, said void volume being defined by the backing layer, the first and the second adhesive zones and the skin surface and wherein the first and the second adhesive zones are capable of moving independently of each others with respect to the lateral plane of the backing layer.

Abstract: A bandage strip includes a plurality of flat adhesive bandage packages of conventional configuration, having sealed therein an adhesive bandage comprising a pad and an adhesive substrate for adhering to a patient and holding the pad in place on the patient's skin. The packages are adhered to an elongated substrate in end-to-end, spaced relation to form a flat, elongated bandage strip, with perforations in the substrate between the packages. A user can dispense a length of substrate, sever it at the perforations, and remove the bandage from the substrate for use in the conventional manner. In another embodiment, a flat adhesive bandage strip comprises an elongated substrate with at least one continuous strip of absorbent material on one side extending in the elongated dimension of the substrate and an adhesive portion adjacent each outside elongated edge of the substrate, with a release liner adhered to the adhesive portion and covering the pad.

Abstract: Pressure sensitive adhesives for use primarily in medical applications are disclosed. The pressure sensitive adhesives are urethane elastomeric adhesives that include a polyurethane polymer and a compatible tackifier and/or compatible plasticizer to achieve an adhesive having a predetermined compliance. The result is a pressure sensitive adhesive for application to skin that can eventually be removed with very little trauma to the skin and with a low pain rating, but which still exhibits very good peel strength when used to construct an article in which the adhesive is adhered to human skin.

Abstract: A medical patch system has a first medical patch including an outer locating ring securable to a surface and an inner patch, separable from the outer locating ring, disposed within the outer locating ring. The medical patch system includes a second medical patch adapted for insertion into the central area bounded by the outer locating ring after the inner patch is separated from the outer locating ring. The second medical patch includes a second outer locating ring securable to the surface, and a second inner patch section, separable from the second outer locating ring, disposed within a second central area bounded by the second outer locating ring. The first and second outer locating rings have adhesive layers for securing the outer locating rings to a surface. The adhesive layers on the respective outer locating rings have different sizes, shapes or patterns to minimize skin irritation.

Abstract: An adhesive bandage is provided with a body portion having a gauze portion and an adhesive portion. The adhesive portion having an adhesive on a first surface of the body portion adapted to adhere to skin. The body portion having a cavity for storing two or more gauze portions, the cavity having a first opening on the first surface for exposing one of the two or more gauze portions to the skin and a second opening on a second surface for removing the exposed gauze portion through the second opening and replacing the exposed gauze portion with another of the two or more gauze portions in the first opening. Also provided are adhesive bandages having a cavity for storing a medicament or a port, each in communication with the gauze portion for providing medicament to the gauze portion.

Abstract: An adhesive patch easily applied to the skin. An adhesive patch 10 according to the present invention includes a support 12, a pressure-sensitive adhesive agent layer 14 provided on one surface of the support, a release sheet 16 which is releasably attached to the pressure-sensitive adhesive agent layer, and a weakened part 20 which is formed in the release sheet, that is for easily dividing the release sheet, and further, a pinching piece forming sheet 18 is fixed so as to cover the weakened part 20 on the release sheet, and portions of the pinching piece forming sheet other than the fixed portions 22 function as pinching pieces 18a and 18b, and in the pinching piece forming sheet as well, a weakened part 20 for easily dividing the release sheet is formed at a position corresponding to the weakened part of the release sheet.

Abstract: A scent emitting patch remains securely attached to the skin of a wearer and is appointed for controlled release of scents. The patch is constructed having an external top layer and backing layer with a skin-contacting portion. The skin-contacting segment contains an adhesive. At least one reservoir comprising pockets or microcapsules containing a scent is disposed in at least one portion of the backing layer. These pockets or microcapsules are operative to rupture upon application of pressure or scratching by the patch wearer. Upon rupture, scent is delivered to the skin to emit aroma. Pockets containing the scent are formed in the backing layer. Microcapsules, if present, are preferably incorporated in the adhesive. A plethora of aromas are provided in the form of a perfume or cologne and correlating shapes can be used to form the patch. Scent is released at the skin-contact interface when pressure is applied ruptures the pockets or microcapsules, permitting controlled release at the wearer's election.

Abstract: A surgical wound closure device comprising multiple layers joined at only one edge of each layer in a book-like arrangement and having opposite unjoined edges, including a substrate having a proximal surface and a distal surface; a drape having a proximal surface and a distal surface, and being disposed proximally to said substrate; and an adhesive layer having a proximal surface and a distal surface; said drape being disposed releasably adherently to said distal surface of said adhesive layer. Also provided is a surgical procedure employing a surgical wound closure device.

Abstract: A protective device having a substantially rigid casing for placement on a patient's skin, wherein the casing has a hollow interior facing the patient's skin and a lip. The casing can be spanned across its hollow interior by a membrane. The casing can have a first adhesive seal attached to a bottom surface of the lip of the casing, and a second adhesive seal attached to the top surface of the lip of the casing.

Abstract: Acrylate adhesive composition comprising N-methacryloyl-3,4-dihydroxyphenylalanine and/or N-acrylol-3,4-dihydroxyphenylalanine. The adhesive composition ensures an adhesion of substrates under moist conditions, in particular a biocompatible and waterproof adhesion to human skin.

Abstract: A device for promoting the clotting of blood comprises a clay material in particle form and a receptacle for containing the clay material. At least a portion of the receptacle is defined by a mesh. Another device comprises a gauze substrate and a clay material disposed on the gauze substrate. Another device is a bandage comprising a substrate, a mesh mounted on the substrate, and particles of a clay material retained in the mesh. A hemostatic sponge comprises a substrate, a hemostatic material disposed on a first surface of the substrate, and a release agent disposed on a second surface of the substrate. The release agent is disposed on the wound-contacting surface of the substrate. When treating a bleeding wound, application of the hemostatic sponge causes at least a portion of the hemostatic material to come into contact with blood through the release agent and through the substrate.

Abstract: A foreskin patch and a fixator for use in circumcision surgery. The foreskin patch (1) is in the form of an elongated strip, having an adhesive surface (11) on one side, and a ventilation structure (12). The ventilation structure comprises a plurality of breather holes or a breathable mesh. The fixator (2) comprises an annular sleeve, which has an accommodation space (21) to accommodate a penis. A plurality of fixing pins (22) are provided on the outer surface of the fixator. The fixing pins are needle-like structures vertically located on the outer surface of the fixator. The fixator is integrally formed from materials absorbable by human body.

Abstract: A vibration dampening device is a patch with one or more step members that have distal ends extending from the patch. The patch is removably engaged or adhered to a wearer's skin. With the patch engaged, the distal ends of the step members have freedom of movement with respect to the patch. The patch optionally may further include one or more wing sections integrally formed therein that also have freedom of movement with respect to the portion of the patch engaged or adhered to skin. Step member and/or wing section movement counteracts longitudinal and/or radial vibrations traveling through soft tissue and musculature to dampen such vibrations.

Abstract: A wound dressing includes an absorbent core defining opposed proximal and distal surfaces including a central portion and a border portion, and a liquid impervious, vapor permeable backing layer connected to the distal surface of the absorbent core. The backing layer defines a border portion extending beyond the periphery of the absorbent core. A skin adherent, perforated facing layer is secured to the proximal surface of the absorbent core. An adhesive layer is applied to at least a proximal segment of the border portion of the backing layer and has greater skin adherence properties than the facing layer.

Abstract: A wound dressing package encloses an adhesive dressing, which has a contact surface and an opposed shielding surface. The contact surface of the adhesive dressing includes a treatment surface and an adhesive surface. The package includes a flexible carrier, which has an inner surface that faces the shielding surface of the adhesive dressing; and a protective cover, which has an inward surface that faces the contact surface of the adhesive dressing. The protective cover is attached to the flexible carrier to enclose the adhesive dressing. The protective cover is stiffer than the flexible carrier, and is configured to split apart adjacent the treatment surface when the wound dressing package is bent with the protective cover in tension.

Abstract: First aid hats/First aid caps are a cost effective and economical method for treating any systemic illness or topical skin condition such as boil, bruise, or burn, using first aid strips, by providing a pouch which provides a means to use medication in the form of cream or gel. The provision of a pouch prevents medication from escaping when applied on the body with an adhesive first aid strip. Thus a measured amount of any medication when applied stays where it is applied and not lost. A ring made of rubber/latex is used to create the said pouch, when placed on the first aid strip.

Abstract: An apparatus, system, and method are disclosed for protection, depressurization, and treatment of a traumatic wound. The disclosed apparatus comprises a flexible patch with an elevated portion configured to accommodate multiple connectors at least one of which is configured to interface with a two-way valve.

Abstract: A medical device comprising a sheath that fits around at least a portion of the circumference of a finger, optionally comprising a pouch for retaining an insert, for supporting and protecting the finger.

Abstract: A wound dressing is made of multiple layers and includes a collection chamber that is in fluid communication with a drainage channel. When applied over a wound, the wound dressing provides protection for the wound while allowing air and fluids to evacuate from the wound through the collection chamber and out through the drainage channel. The wound dressing can include a valve that restricts air and fluids from entering the wound, which is beneficial for treating pneumothorax.

Abstract: The invention relates to an absorbent adhesive body of a foamed pressure sensitive hydrocolloid adhesive comprising one or more water soluble or water swellable hydrocolloids and having gas bubbles incorporated therein, where the gas in the gas bubbles are in direct contact with the pressure sensitive hydrocolloid adhesive and where tan ? for the adhesive in un-foamed form is below 0.35 at 40° C. and 0.001 rad/sec.

Abstract: Liquid hemostatic coating materials comprise a cyanoacrylate monomer and a solvent system comprising a volatile, non-reactive liquid that is non-stinging and non-irritating to a user. The material forms a coating or bandage in the form of a film that when applied and adhered to a surface or to the skin of a user inhibits the application surface from adhering to another surface.

Abstract: A stoma pad configured to cooperate with a fluid handing tube comprises a flexible, resilient, soft annular pad having a generally flat bottom surface and a convex annular wall extending upwardly from the bottom surface, and a circular hole extending through the center of the annular wall and the bottom surface. A stoma pad assembly comprises the stoma pad and a retention, support or holding device for securing the stoma pad on a patient.

Abstract: Devices, bandages, kits and methods are described that can control or regulate the mechanical environment of a wound to ameliorate scar and/or keloid formation. The mechanical environment of a wound includes stress, strain, and any combination of stress and strain. The control of a wound's mechanical environment can be active, passive, dynamic, or static. The devices are configured to be removably secured to a skin surface in proximity to the wound site and shield the wound from endogenous and/or exogenous stress.

Abstract: Various systems, methods and materials are disclosed that enable efficient delivery of an agent into an adhesively adhered article, in which the agent elicits a desired outcome, on demand. This strategy, though general in scope, is also more specifically described with regard to enabling painless or atraumatic removal of products adhering to mammalian tissues such as skin and hair by suitably exploiting the ingress of an appropriate agent or like fluid. Other techniques and articles that aid in the handling or removal of such adhesive products are also disclosed.

Abstract: A full coverage adhesive patch includes a base layer with an extended portion at one side, a first sticking portion and a second sticking portion formed respectively on the circumferential surface of the base layer and top edge of the extended portion, and a cover layer located on the base layer and extended portion. The cover layer is formed at a width mating surface width and height of two lateral sides of a user's finger or toe so that can fully wrap the finger or toe in an annular fashion. When the first and second sticking portions are adhered to the finger or toe, the patch of the invention can provide full coverage and waterproof protection for a wound. The cover layer has parallel first folding line and second folding line and mating first notch and second notch corresponding to the base layer and extended portion to enhance wrapping comfort.

Abstract: This disclosure relates generally to adhesives and particularly to reversible adhesives. This disclosure further relates to generally adhesive articles and particularly to wound dressings comprising such adhesives. The adhesive comprises a core and a shell comprising at least two components. One of the components of the shell comprises a polymer formed by reacting a monomer of a thermally reversible polymer and the other component comprises a polymer formed by reacting a monomer of a polymer of a pressure sensitive adhesive. The wound dressing comprises a substrate and the reversible adhesive, forming a reversible wound dressing. Such wound dressings are particularly suitable for treatment of damaged sensitive tissue, for example wounds formed on a fragile skin.

Abstract: A silicone pressure sensitive adhesive with amphiphilic copolymers for maintaining adhesion in a moist environment. The amphiphilic copolymers for silicone adhesives include at least one silicone moiety and at least one hydrophilic segment. Such adhesives are applicable to securing medical devices to human skin.

Abstract: Devices, bandages, kits and methods are described that can control or regulate the mechanical environment of a wound to ameliorate scar and/or keloid formation. The mechanical environment of a wound includes stress, strain, and any combination of stress and strain. The control of a wound's mechanical environment can be active, passive, dynamic, or static. The devices are configured to be removably secured to a skin surface in proximity to the wound site and shield the wound from endogenous and/or exogenous stress.

Abstract: Disclosed herein are terpolymers and blends prepared from polyester terpolymers that can function as pressure-sensitive adhesives. The disclosed articles can comprise the terpolymer and terpolymer blends coated to a conformable backing member. The terpolymer and terpolymer blends can further comprise a bioactive agent.

Abstract: A patch material which includes a backing material having a water-vapor permeability of 3,000 g/m2·day or more and an adhesive layer having a water-vapor permeability of 5,000 g/m2·day or more, wherein the adhesive layer comprises a polyurethane adhesive obtained by reacting (i) an active hydrogen compound having a number-average molecular weight of 5,000 or more and an average number of functional groups of 2 or more, and having a polyoxyalkylene structure, (ii) an active hydrogen compound having a number-average molecular weight of 1,500 to 5,000 and an average number of functional groups of 1, and having a polyoxyalkylene structure, and (iii) an organic polyisocyanate, wherein an average number of functional groups of all active hydrogen compounds used for obtaining the adhesive is 2 to 2.6, and the content of ethylene oxide units of all active hydrogen compounds in the adhesive is 3 to 8% by weight.

Abstract: A medical dressing for chest wounds, including a one-way valve that can be covered so as to protect against intrusion of airborne contaminants and to prevent passage of fluids in either direction, and including indicia visible using night vision devices but not visible in visible light to the naked eye in some embodiments. The indicia visible using night vision devices may be included in other medical apparatus, as well, so that the medical dressings or other apparatus can be used effectively during darkness, in combat situations, without being seen by enemy combatants not equipped with night vision devices.

Abstract: Apparatus and associated methods for a wound valve assembly provide an annular space extending radially around a central portion of a valve, which valve acts to substantially relieve pressure build up in a thoracic cavity when applied to a thoracic wound. In an illustrative example, the valve assembly may form an annular space that extends radially in all directions around a check valve. In some examples, gasses and exudates may flow substantially radially and/or parallel to the patient's local body. Various embodiments may advantageously provide open fluid communication for the gasses and exudates escaping from the wound when the valve assembly is partially covered (e.g., body armor, clothing, blankets), or when the patient may be laying down on the side of the body with the wound, for example.

Abstract: A hemostatic device for promoting the clotting of blood includes a gauze substrate, a clay material disposed on the gauze substrate, and also a polyol such as glycerol or the like disposed on the gauze substrate to bind the clay material. When the device is used to treat a bleeding wound, at least a portion of the clay material comes into contact with blood emanating from the wound to cause the clotting. A bandage that can be applied to a bleeding wound to promote the clotting of blood includes a flexible substrate and a gauze substrate mounted thereon. The gauze substrate includes a clay material and a polyol. A hemostatic sponge also includes a gauze substrate and a dispersion of hemostatic material and a polyol on a first surface of the substrate.

Abstract: An epidermal positioning mechanism for use with an application to a predetermined epidermal surface. The epidermal positioning mechanism comprises a strip of material having a first end portion of a predetermined shape, a second end portion of a predetermined shape, and middle portion coupling the first end portion to the second end portion. The first end portion and the second end portion each may include a side including an adhesive layer. An overlaying, non-adhesive barrier layer may be located between a portion of the adhesive layer and an end portion.

Abstract: Devices, bandages, kits and methods are described that can control or regulate the mechanical environment of a wound to ameliorate scar and/or keloid formation. The mechanical environment of a wound includes stress, strain, and any combination of stress and strain. The control of a wound's mechanical environment can be active, passive, dynamic, or static. The devices are configured to be removably secured to a skin surface in proximity to the wound site and shield the wound from endogenous and/or exogenous stress.